Product Details

SNP ID
rs201916377
Assay Type
Functionally tested
NCBI dbSNP Submissions
4
Location
Chr.1:16251108 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GAGGAGGACTTAGTGCTGCAGAGGC[C/T]GAGGGGCCTTTGGAGGACATCGCTT
Phenotype
MIM: 609109
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
FBXO42 PubMed Links

Gene Details

Gene
FBXO42
Gene Name
F-box protein 42
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_018994.2 1970 Silent Mutation TCA,TCG S572S NP_061867.1
XM_006710698.3 1970 Silent Mutation TCA,TCG S572S XP_006710761.1
XM_017001502.1 1970 Silent Mutation TCA,TCG S341S XP_016856991.1
XM_017001503.1 1970 Silent Mutation TCA,TCG S341S XP_016856992.1

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